Canonical Allele Identifier: CA775764457

Gene: FN3KRP

Linked Data

• dbSNP Id: rs1287783488
• gnomAD v3: 17-82727932-AAG-A
• gnomAD v4: 17-82727932-AAG-A
• MyVariant Identifiers: chr17:g.80685809_80685810del (hg19) ; chr17:g.82727933_82727934del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727936_82727937del , CM000679.2:g.82727936_82727937del	GRCh38
NC_000017.10:g.80685812_80685813del , CM000679.1:g.80685812_80685813del	GRCh37
NC_000017.9:g.78279101_78279102del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*765_*766del MANE Select	ENSP00000269373.6:n.*765_*766del
ENST00000269373.10:c.*765_*766del	ENSP00000269373.6:n.*765_*766del
ENST00000571594.1:c.53+769_53+770del	ENSP00000459751.1:n.53+769_53+770del
NM_024619.3:c.*765_*766del	NP_078895.2:n.*765_*766del
NR_046408.1:n.1873_1874del
XM_024450948.1:c.*765_*766del	XP_024306716.1:n.*765_*766del
NM_024619.4:c.*765_*766del MANE Select	NP_078895.2:n.*765_*766del
NR_046408.2:n.1873_1874del